Etienne Leveille, MD
Hospital Resident
Research & Publications
Biography
News
Coauthors
Selected Publications
- Metabolic determinants of B-cell selection.Chan LN, Aghania E, Leveille E, Müschen M. Metabolic determinants of B-cell selection. Biochemical Society Transactions 2021, 49: 1467-1478. PMID: 34196360, DOI: 10.1042/BST20201316.
- Genetic Events Inhibiting Apoptosis in Diffuse Large B Cell Lymphoma.Leveille E, Johnson NA. Genetic Events Inhibiting Apoptosis in Diffuse Large B Cell Lymphoma. Cancers 2021, 13 PMID: 33946435, PMCID: PMC8125500, DOI: 10.3390/cancers13092167.
- GCH1 mutations in hereditary spastic paraplegia.Varghaei P, Yoon G, Estiar MA, Veyron S, Leveille E, Dupré N, Trempe JF, Rouleau GA, Gan-Or Z. GCH1 mutations in hereditary spastic paraplegia. Clinical Genetics 2021, 100: 51-58. PMID: 33713342, DOI: 10.1111/cge.13955.
- Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learning.Ramezani M, Mouches P, Yoon E, Rajashekar D, Ruskey JA, Leveille E, Martens K, Kibreab M, Hammer T, Kathol I, Maarouf N, Sarna J, Martino D, Pfeffer G, Gan-Or Z, Forkert ND, Monchi O. Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learning. Scientific Reports 2021, 11: 4917. PMID: 33649398, PMCID: PMC7921412, DOI: 10.1038/s41598-021-84316-4.
- Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7.Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Dion PA, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders : Official Journal Of The Movement Disorder Society 2021 PMID: 33598982, DOI: 10.1002/mds.28528.
- Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease.Ramezani M, Ruskey JA, Martens K, Kibreab M, Javer Z, Kathol I, Hammer T, Cheetham J, Leveille E, Martino D, Sarna JR, Gan-Or Z, Pfeffer G, Ismail Z, Monchi O. Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease. Frontiers In Neurology 2020, 11: 587992. PMID: 33584494, PMCID: PMC7874164, DOI: 10.3389/fneur.2020.587992.
- Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease.Brown EE, Blauwendraat C, Trinh J, Rizig M, Nalls MA, Leveille E, Ruskey JA, Jonvik H, Tan MMX, Bandres-Ciga S, Hassin-Baer S, Brockmann K, Infante J, Tolosa E, Ezquerra M, Ben Romdhan S, Benmahdjoub M, Arezki M, Mhiri C, Hardy J, Singleton AB, Alcalay RN, Gasser T, Grosset DG, Williams NM, Pittman A, Gan-Or Z, Fernandez-Santiago R, Brice A, Lesage S, Farrer M, Wood N, Morris HR. Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. Neurobiology Of Aging 2021, 97: 148.e17-148.e24. PMID: 32873436, PMCID: PMC7762821, DOI: 10.1016/j.neurobiolaging.2020.07.002.
- Use of mobile health technologies for postoperative care in paediatric surgery: A systematic review.Nguyen N, Leveille E, Guadagno E, Kalisya LM, Poenaru D. Use of mobile health technologies for postoperative care in paediatric surgery: A systematic review. Journal Of Telemedicine And Telecare 2020, 1357633X20934682. PMID: 32605411, DOI: 10.1177/1357633X20934682.
- GBA variants in REM sleep behavior disorder: A multicenter study.Krohn L, Ruskey JA, Rudakou U, Leveille E, Asayesh F, Hu MTM, Arnulf I, Dauvilliers Y, Högl B, Stefani A, Monaca CC, Abril B, Plazzi G, Antelmi E, Ferini-Strambi L, Heidbreder A, Boeve BF, Espay AJ, De Cock VC, Mollenhauer B, Sixel-Döring F, Trenkwalder C, Sonka K, Kemlink D, Figorilli M, Puligheddu M, Dijkstra F, Viaene M, Oertel W, Toffoli M, Gigli GL, Valente M, Gagnon JF, Desautels A, Montplaisir JY, Postuma RB, Rouleau GA, Gan-Or Z. GBA variants in REM sleep behavior disorder: A multicenter study. Neurology 2020, 95: e1008-e1016. PMID: 32591474, PMCID: PMC7668554, DOI: 10.1212/WNL.0000000000010042.
- Clinical Characterization of Traumatic Acute Interhemispheric Subdural Hematoma.Léveillé E, Schur S, AlAzri A, Couturier C, Maleki M, Marcoux J. Clinical Characterization of Traumatic Acute Interhemispheric Subdural Hematoma. The Canadian Journal Of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques 2020, 47: 504-510. PMID: 32122420, DOI: 10.1017/cjn.2020.44.
- Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype.Estiar MA, Leveille E, Spiegelman D, Dupre N, Trempe JF, Rouleau GA, Gan-Or Z. Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Molecular Genetics & Genomic Medicine 2020, 8: e1052. PMID: 31944623, PMCID: PMC7057081, DOI: 10.1002/mgg3.1052.
- Triple A syndrome presenting as complicated hereditary spastic paraplegia.Leveille E, Gonorazky HD, Rioux MF, Hazrati LN, Ruskey JA, Carnevale A, Spiegelman D, Dionne-Laporte A, Rouleau GA, Yoon G, Gan-Or Z. Triple A syndrome presenting as complicated hereditary spastic paraplegia. Molecular Genetics & Genomic Medicine 2018, 6: 1134-1139. PMID: 30381913, PMCID: PMC6305671, DOI: 10.1002/mgg3.492.
- Sequencing of the GBA coactivator, Saposin C, in Parkinson disease.Ouled Amar Bencheikh B, Leveille E, Ruskey JA, Spiegelman D, Liong C, Fon EA, Rouleau GA, Dauvilliers Y, Dupre N, Alcalay RN, Gan-Or Z. Sequencing of the GBA coactivator, Saposin C, in Parkinson disease. Neurobiology Of Aging 2018, 72: 187.e1-187.e3. PMID: 30037697, PMCID: PMC6215722, DOI: 10.1016/j.neurobiolaging.2018.06.034.
- Association study of essential tremor genetic loci in Parkinson's disease.Ross JP, Mohtashami S, Leveille E, Johnson AM, Xiong L, Dion PA, Fon E, Dauvilliers Y, Dupré N, Rouleau GA, Gan-Or Z. Association study of essential tremor genetic loci in Parkinson's disease. Neurobiology Of Aging 2018, 66: 178.e13-178.e15. PMID: 29398123, DOI: 10.1016/j.neurobiolaging.2018.01.001.